KR102570158B1 - Manufacturing method of sorghum doenjang and sorghum doenjang using the same - Google Patents
Manufacturing method of sorghum doenjang and sorghum doenjang using the same Download PDFInfo
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- KR102570158B1 KR102570158B1 KR1020200116504A KR20200116504A KR102570158B1 KR 102570158 B1 KR102570158 B1 KR 102570158B1 KR 1020200116504 A KR1020200116504 A KR 1020200116504A KR 20200116504 A KR20200116504 A KR 20200116504A KR 102570158 B1 KR102570158 B1 KR 102570158B1
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- sorghum
- yeast
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- fermenting
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- 235000011684 Sorghum saccharatum Nutrition 0.000 title claims abstract description 124
- 240000006394 Sorghum bicolor Species 0.000 title claims abstract description 121
- 238000004519 manufacturing process Methods 0.000 title claims description 5
- 244000068988 Glycine max Species 0.000 claims abstract description 69
- 235000010469 Glycine max Nutrition 0.000 claims abstract description 69
- 238000000034 method Methods 0.000 claims abstract description 14
- 240000004808 Saccharomyces cerevisiae Species 0.000 claims description 94
- 241000209140 Triticum Species 0.000 claims description 37
- 235000021307 Triticum Nutrition 0.000 claims description 37
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 33
- 240000005979 Hordeum vulgare Species 0.000 claims description 22
- 235000007340 Hordeum vulgare Nutrition 0.000 claims description 22
- 238000002156 mixing Methods 0.000 claims description 19
- 235000013339 cereals Nutrition 0.000 claims description 18
- 150000003839 salts Chemical class 0.000 claims description 14
- 235000013312 flour Nutrition 0.000 claims description 9
- 238000000227 grinding Methods 0.000 claims description 9
- 239000000203 mixture Substances 0.000 claims description 8
- 238000001035 drying Methods 0.000 claims description 7
- 238000004898 kneading Methods 0.000 claims description 3
- 238000000465 moulding Methods 0.000 claims description 3
- 238000007493 shaping process Methods 0.000 claims description 3
- 238000000855 fermentation Methods 0.000 abstract description 61
- 230000004151 fermentation Effects 0.000 abstract description 61
- 150000008442 polyphenolic compounds Chemical class 0.000 abstract description 14
- 235000013824 polyphenols Nutrition 0.000 abstract description 13
- 230000003078 antioxidant effect Effects 0.000 abstract description 6
- 239000003963 antioxidant agent Substances 0.000 abstract description 4
- 210000000936 intestine Anatomy 0.000 abstract description 4
- 108090000790 Enzymes Proteins 0.000 abstract description 2
- 102000004190 Enzymes Human genes 0.000 abstract description 2
- 239000013543 active substance Substances 0.000 abstract description 2
- 230000000694 effects Effects 0.000 abstract description 2
- 208000007536 Thrombosis Diseases 0.000 abstract 1
- 235000013376 functional food Nutrition 0.000 abstract 1
- 244000046052 Phaseolus vulgaris Species 0.000 description 16
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 16
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 16
- 241000894006 Bacteria Species 0.000 description 13
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
- 238000012360 testing method Methods 0.000 description 11
- 230000001953 sensory effect Effects 0.000 description 9
- 235000014655 lactic acid Nutrition 0.000 description 8
- 239000004310 lactic acid Substances 0.000 description 8
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 6
- 238000002835 absorbance Methods 0.000 description 6
- 235000019640 taste Nutrition 0.000 description 6
- 239000002253 acid Substances 0.000 description 5
- 239000012153 distilled water Substances 0.000 description 5
- 239000000843 powder Substances 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 230000002292 Radical scavenging effect Effects 0.000 description 4
- MGJZITXUQXWAKY-UHFFFAOYSA-N diphenyl-(2,4,6-trinitrophenyl)iminoazanium Chemical compound [O-][N+](=O)C1=CC([N+](=O)[O-])=CC([N+]([O-])=O)=C1N=[N+](C=1C=CC=CC=1)C1=CC=CC=C1 MGJZITXUQXWAKY-UHFFFAOYSA-N 0.000 description 4
- HHEAADYXPMHMCT-UHFFFAOYSA-N dpph Chemical compound [O-][N+](=O)C1=CC([N+](=O)[O-])=CC([N+]([O-])=O)=C1[N]N(C=1C=CC=CC=1)C1=CC=CC=C1 HHEAADYXPMHMCT-UHFFFAOYSA-N 0.000 description 4
- KJFMBFZCATUALV-UHFFFAOYSA-N phenolphthalein Chemical compound C1=CC(O)=CC=C1C1(C=2C=CC(O)=CC=2)C2=CC=CC=C2C(=O)O1 KJFMBFZCATUALV-UHFFFAOYSA-N 0.000 description 4
- 238000002791 soaking Methods 0.000 description 4
- 238000010025 steaming Methods 0.000 description 4
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 3
- 241000209072 Sorghum Species 0.000 description 3
- 229920006328 Styrofoam Polymers 0.000 description 3
- 235000006708 antioxidants Nutrition 0.000 description 3
- 239000008261 styrofoam Substances 0.000 description 3
- 229920000742 Cotton Polymers 0.000 description 2
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 2
- 240000007594 Oryza sativa Species 0.000 description 2
- 235000007164 Oryza sativa Nutrition 0.000 description 2
- 240000000111 Saccharum officinarum Species 0.000 description 2
- 235000007201 Saccharum officinarum Nutrition 0.000 description 2
- 150000001413 amino acids Chemical class 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 235000021107 fermented food Nutrition 0.000 description 2
- 235000013305 food Nutrition 0.000 description 2
- LNTHITQWFMADLM-UHFFFAOYSA-N gallic acid Chemical compound OC(=O)C1=CC(O)=C(O)C(O)=C1 LNTHITQWFMADLM-UHFFFAOYSA-N 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 2
- 108090000623 proteins and genes Proteins 0.000 description 2
- 102000004169 proteins and genes Human genes 0.000 description 2
- 238000010298 pulverizing process Methods 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 235000009566 rice Nutrition 0.000 description 2
- 235000019600 saltiness Nutrition 0.000 description 2
- 235000019643 salty taste Nutrition 0.000 description 2
- 235000013555 soy sauce Nutrition 0.000 description 2
- 239000010902 straw Substances 0.000 description 2
- 244000063299 Bacillus subtilis Species 0.000 description 1
- 235000014469 Bacillus subtilis Nutrition 0.000 description 1
- 229920002670 Fructan Polymers 0.000 description 1
- 101710107035 Gamma-glutamyltranspeptidase Proteins 0.000 description 1
- 101710173228 Glutathione hydrolase proenzyme Proteins 0.000 description 1
- IMQLKJBTEOYOSI-GPIVLXJGSA-N Inositol-hexakisphosphate Chemical compound OP(O)(=O)O[C@H]1[C@H](OP(O)(O)=O)[C@@H](OP(O)(O)=O)[C@H](OP(O)(O)=O)[C@H](OP(O)(O)=O)[C@@H]1OP(O)(O)=O IMQLKJBTEOYOSI-GPIVLXJGSA-N 0.000 description 1
- 241000186660 Lactobacillus Species 0.000 description 1
- 235000005135 Micromeria juliana Nutrition 0.000 description 1
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
- IMQLKJBTEOYOSI-UHFFFAOYSA-N Phytic acid Natural products OP(O)(=O)OC1C(OP(O)(O)=O)C(OP(O)(O)=O)C(OP(O)(O)=O)C(OP(O)(O)=O)C1OP(O)(O)=O IMQLKJBTEOYOSI-UHFFFAOYSA-N 0.000 description 1
- 108010020346 Polyglutamic Acid Proteins 0.000 description 1
- 240000002114 Satureja hortensis Species 0.000 description 1
- 235000007315 Satureja hortensis Nutrition 0.000 description 1
- 102000004142 Trypsin Human genes 0.000 description 1
- 108090000631 Trypsin Proteins 0.000 description 1
- 101710162629 Trypsin inhibitor Proteins 0.000 description 1
- 229940122618 Trypsin inhibitor Drugs 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 238000000540 analysis of variance Methods 0.000 description 1
- 230000003178 anti-diabetic effect Effects 0.000 description 1
- 239000003146 anticoagulant agent Substances 0.000 description 1
- 238000011088 calibration curve Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- GVJHHUAWPYXKBD-UHFFFAOYSA-N d-alpha-tocopherol Natural products OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 description 1
- 235000013325 dietary fiber Nutrition 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 238000003113 dilution method Methods 0.000 description 1
- 210000005069 ears Anatomy 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 235000013410 fast food Nutrition 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 235000019634 flavors Nutrition 0.000 description 1
- 229940074391 gallic acid Drugs 0.000 description 1
- 235000004515 gallic acid Nutrition 0.000 description 1
- 102000006640 gamma-Glutamyltransferase Human genes 0.000 description 1
- 229920000370 gamma-poly(glutamate) polymer Polymers 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- GOMNOOKGLZYEJT-UHFFFAOYSA-N isoflavone Chemical compound C=1OC2=CC=CC=C2C(=O)C=1C1=CC=CC=C1 GOMNOOKGLZYEJT-UHFFFAOYSA-N 0.000 description 1
- CJWQYWQDLBZGPD-UHFFFAOYSA-N isoflavone Natural products C1=C(OC)C(OC)=CC(OC)=C1C1=COC2=C(C=CC(C)(C)O3)C3=C(OC)C=C2C1=O CJWQYWQDLBZGPD-UHFFFAOYSA-N 0.000 description 1
- 235000008696 isoflavones Nutrition 0.000 description 1
- AIHDCSAXVMAMJH-GFBKWZILSA-N levan Chemical group O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)OC[C@@H]1[C@@H](O)[C@H](O)[C@](CO)(CO[C@@H]2[C@H]([C@H](O)[C@@](O)(CO)O2)O)O1 AIHDCSAXVMAMJH-GFBKWZILSA-N 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000002609 medium Substances 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 229920001542 oligosaccharide Polymers 0.000 description 1
- 150000002482 oligosaccharides Chemical class 0.000 description 1
- 239000002504 physiological saline solution Substances 0.000 description 1
- 229940068041 phytic acid Drugs 0.000 description 1
- 235000002949 phytic acid Nutrition 0.000 description 1
- 239000000467 phytic acid Substances 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000001397 quillaja saponaria molina bark Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 229930182490 saponin Natural products 0.000 description 1
- 150000007949 saponins Chemical class 0.000 description 1
- 235000017709 saponins Nutrition 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 239000010421 standard material Substances 0.000 description 1
- 239000011550 stock solution Substances 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 230000002537 thrombolytic effect Effects 0.000 description 1
- 238000004448 titration Methods 0.000 description 1
- 235000010384 tocopherol Nutrition 0.000 description 1
- 229960001295 tocopherol Drugs 0.000 description 1
- 229930003799 tocopherol Natural products 0.000 description 1
- 239000011732 tocopherol Substances 0.000 description 1
- 239000012588 trypsin Substances 0.000 description 1
- 239000002753 trypsin inhibitor Substances 0.000 description 1
- 239000006150 trypticase soy agar Substances 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- GVJHHUAWPYXKBD-IEOSBIPESA-N α-tocopherol Chemical compound OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-IEOSBIPESA-N 0.000 description 1
Classifications
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L7/00—Cereal-derived products; Malt products; Preparation or treatment thereof
- A23L7/10—Cereal-derived products
- A23L7/104—Fermentation of farinaceous cereal or cereal material; Addition of enzymes or microorganisms
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L11/00—Pulses, i.e. fruits of leguminous plants, for production of food; Products from legumes; Preparation or treatment thereof
- A23L11/50—Fermented pulses or legumes; Fermentation of pulses or legumes based on the addition of microorganisms
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L27/00—Spices; Flavouring agents or condiments; Artificial sweetening agents; Table salts; Dietetic salt substitutes; Preparation or treatment thereof
- A23L27/40—Table salts; Dietetic salt substitutes
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L5/00—Preparation or treatment of foods or foodstuffs, in general; Food or foodstuffs obtained thereby; Materials therefor
- A23L5/10—General methods of cooking foods, e.g. by roasting or frying
- A23L5/13—General methods of cooking foods, e.g. by roasting or frying using water or steam
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23P—SHAPING OR WORKING OF FOODSTUFFS, NOT FULLY COVERED BY A SINGLE OTHER SUBCLASS
- A23P30/00—Shaping or working of foodstuffs characterised by the process or apparatus
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2002/00—Food compositions, function of food ingredients or processes for food or foodstuffs
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2300/00—Processes
- A23V2300/10—Drying, dehydrating
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2300/00—Processes
- A23V2300/31—Mechanical treatment
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A40/00—Adaptation technologies in agriculture, forestry, livestock or agroalimentary production
- Y02A40/90—Adaptation technologies in agriculture, forestry, livestock or agroalimentary production in food processing or handling, e.g. food conservation
Abstract
콩을 이용한 장류는 각종 생리활성물질, 항산화물질 및 혈전용해 효소를 다량 함유하고 있기 때문에, 기능성 식품으로서 그 중요하다. 이와 같은 효과에도 불구하고 기존의 장을 발효시키는데 시간이 오래걸리는 단점이 존재하였다. 이에 본 발명에서는 장을 발효시키는 시간을 단축시키고, 총폴리페놀 함량, 항산화효과 등이 우수한 수수 속성장을 제조하는 방법을 제공하는데 그 목적이 있다.Soybean pastes are important as functional foods because they contain a large amount of various physiologically active substances, antioxidants, and blood clot-dissolving enzymes. Despite such an effect, there was a disadvantage that it took a long time to ferment the existing intestine. Accordingly, an object of the present invention is to shorten the fermentation time of the intestine and provide a method for preparing sorghum soybean paste with excellent total polyphenol content and antioxidant effect.
Description
본 발명은 수수를 함유하는 수수 속성장 제조방법 및 이를 이용한 수수 속성장에 관한 것이다. The present invention relates to a method for preparing a sorghum accelerator containing sorghum and a sorghum accelerator using the same.
콩을 원료로 한 우리나라의 대표적인 발효식품으로서, 간장, 청국장 등과 함께 된장과 고추장은 오늘날까지 상용되어 온 전통 장류 중의 하나이며, 곡류를 주식으로 하는 우리 민족에게 결핍되기 쉬운 필수 아미노산 및 지방산을 공급시켜 주는 식품으로서 중요한 역할을 담당하여 왔다. 발효시킨 콩은 삶은 콩을 볏짚에 붙어있는 바실러스 서브틸리스(Bacillus subtilis)를 이용하여 발효시켜 만든 것으로서, 원료 콩의 당질과 단백질에서 유래된 레반형 프룩탄(levan form fructan)과 폴리글루타메이트(polyglutamate)의 혼합물질인 점질물을 다량 생성하며, 이렇게 발효시킨 콩을 사용하여 제조한 발효 된장과 발효 고추장은 재래식 메주로 만든 된장이나 고추장, 또 코오지(쌀이나 밀을 황국균으로 전분을 분해 시킨 누룩)를 섞어 띄운 개량메주로 만든 된장이나, 개량메주로 만든 된장과 혼합하여 제조한 장보다 단백질이 인체 내로 흡수되기 쉬운 아미노산으로 완전하게 분해되어 있는, 아미노산 수치가 월등히 높은 양질의 콩 발효식품인 것이다. 최근 많은 연구자들에 의하여 콩발효물 내에 포함된 활성성분 및 그 역할이 밝혀지고 있는바, 발효시킨 콩은 콩에서 기인된 이소플라본(isoflavone), 피트산(phytic acid), 사포닌(saponin), 트립신저해제(trypsininhibitor), 토코페롤(tocopherol), 불포화지방산, 식이섬유, 올리고당, γ글루타밀트랜스펩티다제(γγ등의 각종 생리활성물질, 항산화물질 및 혈전용해 효소를 다량 함유하고 있기 때문에, 기능성 식품으로서 중요하다. 이와 같은 효과에도 불구하고 기존의 장을 발효시키는데 시간이 오래걸리는 단점이 존재하였다. As Korea's representative fermented foods made from soybeans, soybean paste and gochujang, along with soy sauce and cheonggukjang, are one of the traditional soybeans that have been commercially used to this day. It has played an important role as a food. Fermented soybeans are made by fermenting boiled soybeans using Bacillus subtilis attached to rice straw, and levan form fructan and polyglutamate derived from sugar and protein of raw soybeans. ), and fermented soybean paste and fermented gochujang prepared using soybeans fermented in this way are soybean paste or gochujang made from traditional fermented soybeans, and koji (nuruk, which is a yeast that decomposes rice or wheat with Hwanggukgyun) It is a high-quality soybean fermented food with a much higher amino acid level than soybean paste made from mixed fermented soybean paste or soybean paste made by mixing soybean paste with improved fermented soybean paste, in which protein is completely decomposed into amino acids that are easily absorbed into the body. Recently, active ingredients and their roles in fermented soybean products have been revealed by many researchers. Fermented soybeans contain isoflavone, phytic acid, saponin, and trypsin derived from soybeans. As it contains a large amount of various physiologically active substances such as trypsininhibitor, tocopherol, unsaturated fatty acids, dietary fiber, oligosaccharide, γ-glutamyltranspeptidase (γγ), antioxidants and thrombolytic enzymes, Important: Despite such an effect, there was a disadvantage that it took a long time to ferment the existing intestine.
본 발명은 상기한 문제점을 해결하기 위한 것으로, 장을 발효시키는 시간을 단축시키고, 총폴리페놀 함량, 항산화효과 등이 우수한 수수 속성장을 제조하는 방법을 제공하는데 그 목적이 있다.The present invention is to solve the above problems, and an object of the present invention is to provide a method for preparing sorghum soybean paste with excellent total polyphenol content, antioxidant effect, etc. by shortening the fermentation time of intestine.
본 발명은 불린 콩을 증자하는 단계, 수수가 첨가된 곡류를 분쇄하는 단계, 분쇄된 상기 곡류를 물과 혼합하며 반죽하고 성형하는 단계, 반죽된 상기 곡류를 발효하여 누룩을 만드는 단계, 햇볕 또는 건조기를 이용하여 누룩을 겉말림하는 단계, 상기 누룩을 분쇄하고, 분쇄된 상기 누룩에 메주가루, 소금 및 물을 혼합하여 속성장을 제조하는 단계 및 상기 속성장을 발효하는 단계를 포함하는 수수 속성장 제조방법을 제공한다.The present invention is a step of steaming soaked beans, grinding grains with sorghum added thereto, mixing the pulverized grains with water, kneading and shaping, fermenting the kneaded grains to make yeast, sunlight or dryer Sorghum fastening method comprising the steps of over-rolling yeast using, crushing the yeast, mixing fermented soybean flour, salt and water with the crushed yeast to prepare a quick-drying paste, and fermenting the quick-drying paste. A manufacturing method is provided.
본 발명의 일 실시예에 있어서, 상기 증자하는 단계는 대두를 30분 내지 3시간 불리는 단계, 대두 중량 대비 1.2배 내지 2.5배의 물을 첨가하는 단계 및 80℃ 내지 140℃에서 15분 내지 45분간 증자하는 단계를 포함할 수 있다.In one embodiment of the present invention, the step of increasing the soybeans is soaking the soybeans for 30 minutes to 3 hours, adding 1.2 to 2.5 times the amount of water compared to the weight of the soybeans, and 15 to 45 minutes at 80 ° C to 140 ° C. It may include a step of increasing.
본 발명의 일 실시예에 있어서, 상기 수수가 첨가된 곡류를 분쇄하는 단계는, 통밀 또는 보리 중 어느 하나 이상을 더 포함할 수 있다.In one embodiment of the present invention, the step of grinding the grains to which sorghum is added may further include any one or more of whole wheat or barley.
본 발명의 일 실시예에 있어서, 상기 성형하는 단계는 수수, 통밀 또는 보리 중 어느 하나 이상이 첨가된 시료와 물을 1 : 0.25 내지 1 : 2.0의 비율로 혼합하는 단계 및 상기 혼합물을 고르게 분쇄하는 단계를 포함할 수 있다.In one embodiment of the present invention, the molding step is mixing a sample to which one or more of sorghum, whole wheat or barley is added and water at a ratio of 1: 0.25 to 1: 2.0 and evenly pulverizing the mixture steps may be included.
본 발명의 일 실시예에 있어서, 상기 누룩을 발효하는 단계는 상기 곡류를 온도 20℃ 내지 40℃, 습도 40% 내지 90%에서 3일 내지 24일 발효하는 단계일 수 있다.In one embodiment of the present invention, the step of fermenting the yeast may be a step of fermenting the grains at a temperature of 20 ° C to 40 ° C and a humidity of 40% to 90% for 3 to 24 days.
본 발명의 일 실시예에 있어서, 상기 혼합하는 단계는 소금 100중량부 내지 300중량부, 물 700중량부 내지 1500중량부, 메주가루 250중량부 내지 800중량부 및 누룩 50중량부 내지 450중량부를 혼합하는 단계일 수 있다.In one embodiment of the present invention, the mixing step is 100 parts by weight to 300 parts by weight of salt, 700 parts by weight to 1500 parts by weight of water, 250 parts by weight to 800 parts by weight of meju powder, and 50 parts by weight to 450 parts by weight of yeast. It may be a mixing step.
본 발명의 일 실시예에 있어서, 상기 속성장을 발효하는 단계는 20℃ 내지 40℃에서 20일 내지 40일 발효하는 단계일 수 있다.In one embodiment of the present invention, the step of fermenting the fast growth may be a step of fermenting at 20 ° C to 40 ° C for 20 to 40 days.
본 발명은 상기 수수 속성장 제조방법에 의해 제조된 수수 속성장을 제공한다.The present invention provides a sorghum fastening powder prepared by the method for preparing sorghum fastening powder.
총폴리페놀 함량과 항당뇨 효과가 우수한 수수를 이용한 장류를 제조하여 향미가 우수하고, 건강증진에 도움이 될 수 있다.Soybean paste prepared using sorghum, which has excellent total polyphenol content and antidiabetic effect, has excellent flavor and can help promote health.
본 발명은 다양한 변경을 가할 수 있고 여러 가지 형태를 가질 수 있는 바, 특정 실시예들을 도면에 예시하고 본문에 상세하게 설명하고자 한다. 그러나, 이는 본 발명을 특정한 개시 형태에 대해 한정하려는 것이 아니며, 본 발명의 사상 및 기술 범위에 포함되는 모든 변경, 균등물 내지 대체물을 포함하는 것으로 이해되어야 한다. 본 발명의 실시예는 당업계에서 통상의 지식을 가진 자에게 본 발명을 보다 완전하게 설명하기 위해 제공되는 것이다.Since the present invention may have various changes and various forms, specific embodiments are illustrated in the drawings and described in detail in the text. However, it should be understood that this is not intended to limit the present invention to the specific disclosed form, and includes all modifications, equivalents, and substitutes included in the spirit and scope of the present invention. The embodiments of the present invention are provided to more completely explain the present invention to those skilled in the art.
본 명세서에 기재된 용어, 기술 등은 특별한 한정이 없는 한, 본 발명이 속하는 기술 분야에서 일반적으로 사용되는 의미로 사용된다.Terms, techniques, and the like described in this specification are used in the meaning generally used in the technical field to which the present invention belongs unless there is a special limitation.
본 발명에서 사용되는 수수는 높이 1.5∼이다. 표면은 굳고 흰색의 납질물이 있으며 속이 차 있다. 줄기에는 10∼개의 마디가 있고 줄기 끝에 이삭이 달린다. 잎은 마주나고 길이 50∼너비 5cm 정도로 1줄기에 10개 정도 달린다. 처음에는 잎과 줄기가 녹색이나 차츰 붉은 갈색으로 변한다.The sorghum used in the present invention is 1.5 to 1.5 in height. The surface is hard, white waxy, and the inside is full. There are 10 to 10 nodes on the stem, and ears hang at the end of the stem. Leaves are opposite, about 10 on one stem, 50 to 5 cm wide. At first, the leaves and stems are green, but gradually turn reddish brown.
본 발명은 불린 콩을 증자하는 단계, 수수가 첨가된 곡류를 분쇄하는 단계, 분쇄된 상기 곡류를 물과 혼합하며 반죽하고 성형하는 단계, 반죽된 상기 곡류를 발효하여 누룩을 만드는 단계, 햇볕 또는 건조기를 이용하여 누룩을 겉말림하는 단계, 상기 누룩을 분쇄하고, 분쇄된 상기 누룩에 메주가루, 소금 및 물을 혼합하여 속성장을 제조하는 단계 및 상기 속성장을 발효하는 단계를 포함하는 수수 속성장 제조방법을 제공한다.The present invention is a step of steaming soaked beans, grinding grains with sorghum added thereto, mixing the pulverized grains with water, kneading and shaping, fermenting the kneaded grains to make yeast, sunlight or dryer The sorghum fastening process comprising the steps of drying the yeast by using, crushing the yeast, mixing soybean flour, salt and water with the crushed yeast to prepare a fastening paste, and fermenting the fastening yeast. A manufacturing method is provided.
본 발명의 일 실시예에 있어서, 상기 증자하는 단계는 대두를 30분 내지 3시간 불리는 단계, 대두 중량 대비 1.2배 내지 2.5배의 물을 첨가하는 단계 및 80℃ 내지 140℃에서 15분 내지 45분간 증자하는 단계를 포함할 수 있다. 그러나 이에 한정되는 것은 아니며, 대두를 불리는 목적, 증자하는 목적을 달성할 수 있다면 온도 및 시간 범위에 한정되지 않는다.In one embodiment of the present invention, the step of increasing the soybeans is soaking the soybeans for 30 minutes to 3 hours, adding 1.2 to 2.5 times the amount of water compared to the weight of the soybeans, and 15 to 45 minutes at 80 ° C to 140 ° C. It may include a step of increasing. However, it is not limited thereto, and it is not limited to the temperature and time range as long as the purpose of soybean soaking and the purpose of steaming can be achieved.
본 발명의 일 실시예에 있어서, 수수가 첨가된 누룩을 분쇄하는 단계는, 통밀 또는 보리 중 어느 하나 이상을 더 포함할 수 있다. 그러나 이에 한정되는 것은 아니며 다른 작물을 포함하여 누룩을 제조할 수도 있다.In one embodiment of the present invention, the step of grinding the yeast to which sorghum is added may further include any one or more of whole wheat or barley. However, it is not limited thereto, and yeast may be produced including other crops.
본 발명의 일 실시예에 있어서, 상기 성형하는 단계는 수수, 통밀 또는 보리 중 어느 하나 이상이 첨가된 시료와 물을 1 : 0.25 내지 1 : 2.0의 비율로 혼합하는 단계 및 상기 혼합물을 고르게 분쇄하는 단계를 포함할 수 있다. 상기 분쇄하는 단계는 믹서기를 이용하여 수행될 수도 있고, 빻는 방식으로 수행될 수도 있으며, 맷돌로 수행될 수도 있다. 그러나 이에 한정되는 것은 아니다.In one embodiment of the present invention, the molding step is mixing a sample to which one or more of sorghum, whole wheat or barley is added and water at a ratio of 1: 0.25 to 1: 2.0 and evenly pulverizing the mixture steps may be included. The crushing may be performed using a blender, may be performed in a grinding method, or may be performed with a millstone. However, it is not limited thereto.
본 발명의 일 실시예에 있어서, 상기 누룩을 발효하는 단계는 상기 곡류를 온도 20℃ 내지 40℃, 습도 40% 내지 90%에서 3일 내지 24일 발효하는 단계일 수 있다. 그러나 이에 한정되는 것은 아니며, 상기 곡류를 발효하여 누룩을 만드는 목적을 달성할 수 있다면 다른 온도범위, 다른 습도범위 및 다른 기간으로 수행될 수도 있다.In one embodiment of the present invention, the step of fermenting the yeast may be a step of fermenting the grains at a temperature of 20 ° C to 40 ° C and a humidity of 40% to 90% for 3 to 24 days. However, it is not limited thereto, and if it is possible to achieve the purpose of making yeast by fermenting the grains, it may be performed in other temperature ranges, other humidity ranges and other periods.
본 발명의 일 실시예에 있어서, 상기 혼합하는 단계는 소금 100중량부 내지 300중량부, 물 700중량부 내지 1500중량부, 메주가루 250중량부 내지 800중량부 및 누룩 50중량부 내지 450중량부를 혼합하는 단계일 수 있다. 그러나 이에 한정되는 것은 아니며, 사용자의 기호에 따라, 각 함량을 달리할 수도 있다.In one embodiment of the present invention, the mixing step is 100 parts by weight to 300 parts by weight of salt, 700 parts by weight to 1500 parts by weight of water, 250 parts by weight to 800 parts by weight of meju powder, and 50 parts by weight to 450 parts by weight of yeast. It may be a mixing step. However, it is not limited thereto, and each content may be different according to the user's preference.
본 발명의 일 실시예에 있어서, 상기 속성장을 발효하는 단계는 20℃ 내지 40℃에서 20일 내지 40일 발효하는 단계일 수 있다. 그러나 이에 한정되는 것은 아니며, 발효의 목적을 달성할 수 있다면 다른 온도범위 및 다른 기간으로 수행될 수도 있다.In one embodiment of the present invention, the step of fermenting the fast growth may be a step of fermenting at 20 ° C to 40 ° C for 20 to 40 days. However, it is not limited thereto, and fermentation may be performed in other temperature ranges and other periods if the purpose of fermentation can be achieved.
상기 수수 속성장 제조방법에 의해 제조된 수수 속성장을 제공할 수 있다. It is possible to provide a sorghum properties sheet prepared by the method for preparing a sorghum properties sheet.
<실험예><Experimental example>
[누룩 및 속성장 제조][Manufacture of Nuruk and Ingredients]
본 발명에 따른, 누룩은 대두를 1시간 불린 후, 대두 중량 대비 1.5배의 물을 넣고, 고압멸균기(autoclave)에서 121℃로 30분간 증자하여 사용하였다. 수수, 통밀 또는 보리가 첨가된 곡류는 믹서기에서 30초간 분쇄하여 200g의 물을 조금씩 첨가하며, 고르게 치댄 후 물기 있는 면보에 넣어 압력을 가하여 으깨었다. 으깨진 곡류를 직사각형 모양으로 성형하고, 지푸라기를 깐 스티로폼 상자에 넣었다. 이후, 스티로폼에 넣은 곡류를 온도 33℃습도 70%에서 1주일 발효하여 누룩을 제조한 후 24시간 햇볕에서 겉말림하였다. Nuruk according to the present invention was used by soaking soybeans for 1 hour, adding 1.5 times the amount of water relative to the weight of soybeans, and steaming in an autoclave at 121 ° C. for 30 minutes. Grains to which sorghum, whole wheat or barley were added were ground in a blender for 30 seconds, 200 g of water was added little by little, kneaded evenly, and then put in a damp cotton cloth and crushed by applying pressure. The crushed grain was molded into a rectangular shape and placed in a Styrofoam box lined with straw. Thereafter, the grains put in Styrofoam were fermented for 1 week at a temperature of 33 ° C and a humidity of 70% to prepare yeast, and then dried in the sun for 24 hours.
수수 콩알 누룩은 물에 씻어 체에서 물기를 제거한 후 고압멸균기(autoclave)에서 121℃로 15분간 증자하여 사용하였다. 증자한 수수를 35℃로 식힌 후 황국균을 중량의 3% 첨가하여 섞는다. 젖은 면보에 황국균이 첨가된 수수를 넣고 감싼 후 스티로폼 상자에 넣어 온도 30℃습도 80%에서 72시간 발효하여 수수 통알 누룩을 제조한 후 24시간 햇볕에서 겉말림하였다.The sorghum soybean nuruk was washed in water, drained from a sieve, and then steamed in an autoclave at 121 ° C. for 15 minutes and used. After cooling the steamed sorghum to 35 ℃, add 3% of the weight of Hwanggukgyun and mix. After putting sorghum to which Hwanggukgyun was added to a wet cotton cloth and wrapping it, it was put in a Styrofoam box and fermented for 72 hours at a temperature of 30 ° C and a humidity of 80% to prepare whole sorghum nuruk, which was then dried in the sun for 24 hours.
하기 표 1은 시료에 따른 누룩제조 시의 원료 배합비율을 나타낸 표이다(단위 g).Table 1 below is a table showing the mixing ratio of raw materials when producing yeast according to the sample (unit g).
표 1에서 1번 누룩 내지 7번 누룩은 자연발효하였으며, 8번 누룩은 황국균을 접종하여 사용하였다.표 1에 나타난 바와 같이, 시료는 총 600g을 이용하였으며, 대두 및 비도정 수수(콩알)를 이용한 누룩의 경우 900g의 물을 첨가하였으며, 나머지 누룩의 경우 물을 200g 첨가하여 제조하였다.In Table 1, Nuruk No. 1 to No. 7 were naturally fermented, and Nuruk No. 8 was inoculated with Hwanggukgyun and used. In the case of the used yeast, 900 g of water was added, and in the case of the remaining yeast, 200 g of water was added.
[속성장 분석방법] [Rapid growth analysis method]
속성장 시료 50 g을 취하여 증류수 200 mL를 넣고 300rpm, 3시간 진탕추출 하였고, 이를 8,000 rpm, 4℃에서 20분간 원심분리(Supra 22K, Hanil Science Industrial Co., Gimpo, Korea) 하였다. 상등액을 취하여 감압 여과한 뒤 pH 및 산도, 환원당, 아미노태질소 함량, 항산화도 측정(DPPH)의 분석 시료로 사용하였다.50 g of the rapid field sample was added to 200 mL of distilled water, shaken and extracted at 300 rpm for 3 hours, and centrifuged at 8,000 rpm and 4 ° C for 20 minutes (Supra 22K, Hanil Science Industrial Co., Gimpo, Korea). After taking the supernatant and filtering under reduced pressure, it was used as an analysis sample for measuring pH, acidity, reducing sugar, amino nitrogen content, and antioxidant level (DPPH).
총폴리페놀 추출은 된장 10 g에 증류수 20mL를 넣고 300rpm, 3시간 진탕추출 하였고, 이를 8,000 rpm, 4℃에서 20분간 원심분리(Supra 22K, Hanil Science Industrial Co., Gimpo, Korea)하였다.For total polyphenol extraction, 20 mL of distilled water was added to 10 g of soybean paste, shake-extracted at 300 rpm for 3 hours, and centrifuged at 8,000 rpm and 4 ° C for 20 minutes (Supra 22K, Hanil Science Industrial Co., Gimpo, Korea).
[누룩 종류에 따른 속성장의 품질특성][Quality Characteristics of Instant Nuruk According to Types of Nuruk]
표 2는 누룩 종류에 따른 속성장의 제조 원료 배합비율을 나타낸 표이다(단위 g).Table 2 is a table showing the blending ratio of raw materials for rapid growth according to the type of yeast (unit g).
속성장은 제조한 누룩을 분쇄하여 상기 표 2의 배합비율대로 메주가루, 소금 및 물을 혼합한 후, 발효온도 29.4℃에서 28일간 발효시키면서 품질특성을 조사하였다.비도정 수수(콩알)는 물 1100g, 소금 200g, 메주가루 630g 및 누룩 70g을 첨가하여 제조하였다. 이와 달리 나머지 시료의 경우, 물 1200g, 소금 200g, 메주가루 720g 및 누룩 80g을 첨가하여 제조하였다. The quality characteristics of soybean paste were pulverized and fermented for 28 days at a fermentation temperature of 29.4 ° C. , prepared by adding 200 g of salt, 630 g of fermented soybean flour, and 70 g of nuruk. Unlike this, the remaining samples were prepared by adding 1200 g of water, 200 g of salt, 720 g of fermented soybean flour, and 80 g of nuruk.
[누룩 종류에 따른 속성장의 수분함량 변화][Changes in Moisture Content of Instant Nuruk According to Types of Nuruk]
표 3은 상이한 종류의 누룩으로 제조된 속성장을 4주간 발효하여 4주간의 수분함량 변화를 표로 나타낸 것이다.Table 3 shows the change in moisture content for 4 weeks by fermenting fast yeast made with different types of yeast for 4 weeks.
본 발명에 따른 속성장의 수분, pH, 총산은 AOAC법에 따라 측정하였다. 수분은 상압 가열 건조법을 사용하였으며, 발효 과정 중의 pH는 추출시료 10 mL를 취하여 pH 미터(Sartorius, Goettingen, Germany)로 측정하였다. 총산은 추출 시료 10 mL에 DW 20 mL를 넣어 1% 페놀프탈레인 2~3 방울 넣고 0.1 N NaOH 용액으로 pH 8.2~8.3이 될 때까지 적정하였다. 적정에 소비된 0.1 N NaOH 용액의 mL수를 젖산으로 환산하여 나타내었다. Moisture, pH, and total acid of the rapid field according to the present invention were measured according to the AOAC method. Moisture was measured by atmospheric pressure heating and drying, and pH during fermentation was measured with a pH meter (Sartorius, Goettingen, Germany) by taking 10 mL of the extracted sample. For total acid, add 20 mL of DW to 10 mL of the extracted sample, add 2 to 3 drops of 1% phenolphthalein, and titrate with 0.1 N NaOH solution until the pH is 8.2 to 8.3. The number of mL of 0.1 N NaOH solution consumed for titration was expressed in terms of lactic acid.
발효 초기의 수분함량은 57.44중량% 내지 61.04중량%의 범위에 속하였으며, 발효가 경과함에 따라 감소하여 발효 후 4주가 경과한 경우, 52.39중량% 내지 57.63중량%의 범위에 속하였다. 발효 초기에는 비도정 수수의 수분함량이 가장 높았고, 도정수수의 수분함량이 가장 낮았다. 발효 후 4주가 경과한 경우, 비도정 수분함량이 가장 높았으며, 수수+대두의 수분함량이 가장 낮았다. 발효 전과 발효 4주 경과 후의 수분함량 차이는 수수+대두가 5.45중량%로 가장 큰 차이를 나타냈으며, 수수+보리가 2.78로 가장 작은 차이를 나타내었다.The moisture content at the beginning of fermentation was in the range of 57.44% by weight to 61.04% by weight, and decreased as fermentation progressed, and was in the range of 52.39% by weight to 57.63% by weight when 4 weeks passed after fermentation. In the initial stage of fermentation, unpolished sorghum had the highest moisture content, and polished sorghum had the lowest moisture content. When 4 weeks had elapsed after fermentation, the unpeeled moisture content was the highest, and the moisture content of sorghum + soybean was the lowest. As for the difference in water content before fermentation and after 4 weeks of fermentation, sorghum + soybean showed the largest difference at 5.45% by weight, and sorghum + barley showed the smallest difference at 2.78.
[누룩 종류에 따른 속성장의 pH와 총산 변화][Changes in pH and total acidity of fast-acting yeast depending on the type of yeast]
표 4는 상이한 종류의 누룩으로 제조된 속성장을 4주간 발효하여 4주간의 pH와 총산을 분석한 결과를 표로 나타낸 표이다. Table 4 is a table showing the results of analyzing the pH and total acid for 4 weeks by fermenting fast yeast prepared with different types of yeast for 4 weeks.
(%)Total
(%)
(%)Total
(%)
(%)Total
(%)
(%)Total
(%)
(%)Total
(%)
pH는 발효 초기 6.00 내지 6.25에서 발효기간이 경과함에 따라, 발효 4주 후 5.54 내지 5.73으로 감소하였다. 총산 함량은 발효 초기 0.57중량% 내지 0.74중량%에서 발효 4주 경과 후 1.32중량% 내지 1.61중량%로 증가하였다. 발효 4주차 수수+통밀 누룩을 첨가한 속성장이 없는 pH는 가장 낮고 총산은 가장 높은 값을 보였다.The pH decreased from 6.00 to 6.25 at the beginning of fermentation to 5.54 to 5.73 after 4 weeks of fermentation as the fermentation period elapsed. The total acid content increased from 0.57 wt% to 0.74 wt% at the initial stage of fermentation to 1.32 wt% to 1.61 wt% after 4 weeks of fermentation. In the 4th week of fermentation, sorghum + whole wheat nuruk added the lowest pH value and the highest total acid value without the fast fermentation.
[누룩 종류에 따른 속성장의 명도변화][Change in the brightness of the property field according to the type of yeast]
표 5는 상이한 종류의 누룩으로 제조된 속성장을 4주간 발효하여 4주간의 명도변화를 표로 나타낸 것이다. Table 5 shows the change in brightness for 4 weeks by fermenting fast yeast made with different types of yeast for 4 weeks.
누룩 종류에 따른 속성장의 발효기간에 따른 명도변화를 분석한 결과 발효초기 48.62 내지 50.30에서 발효 기간이 경과함에 따라 41.06 내지 44.38로 감소하는 경향을 보였다. 발효 전후의 명도 차이에 있어서, 도정수수를 누룩으로 사용한 경우가 7.74로 가장 컸으며, 대두를 누룩으로 사용한 경우가 5.3으로 가장 작게 나타났다.As a result of analyzing the change in brightness according to the fermentation period of the quick-drying yeast according to the type of yeast, it showed a tendency to decrease from 48.62 to 50.30 at the beginning of fermentation to 41.06 to 44.38 as the fermentation period elapsed. Regarding the difference in lightness before and after fermentation, the case where milled sorghum was used as yeast was the largest at 7.74, and the case where soybean was used as yeast was the smallest at 5.3.
[누룩 종류에 따른 속성장의 적색도(a) 변화][Changes in the redness (a) of the property field according to the type of yeast]
표 6은 상이한 종류의 누룩으로 제조된 속성장을 4주간 발효하여 4주간의 적색도(a) 변화를 표로 나타낸 것이다.Table 6 shows the change in redness (a) for 4 weeks by fermenting fast yeast made with different types of yeast for 4 weeks.
색도 측정은 색도색차계(CM-3500d, Minolta, Tokyo, Japan)를 이용하여 명도는 L값 (lightness), 적색도는 a값(redness), 황색도는 b값(yellowness)으로 비교하였다. 된장 10 g을 페트리디쉬에 고르게 담고 3회 측정한 값의 평균값으로 나타내었으며, 표준백판의 값은 L=96.89, a=-0.07, b=-0.18이었다.Chromaticity was measured using a chromaticity colorimeter (CM-3500d, Minolta, Tokyo, Japan), and compared lightness with L value (lightness), redness with a value (redness), and yellowness with b value (yellowness). 10 g of soybean paste was evenly placed in a petri dish and expressed as the average value of three measurements. The values of the standard white plate were L = 96.89, a = -0.07, b = -0.18.
누룩 종류에 따른 속성장의 발효기간에 따른 적색도 변화를 분석한 결과 발효초기 8.06 내지 8.95에서 발효 기간이 경과함에 따라 7.47 내지 8.93로 변하였다. 상기 표 6에 나타난 바와 같이 속성장이 발효되는 동안, 적색도의 큰 차이는 없는 것으로 나타났다.As a result of analyzing the change in redness according to the fermentation period of the quick yeast according to the type of yeast, it changed from 8.06 to 8.95 at the beginning of fermentation to 7.47 to 8.93 as the fermentation period elapsed. As shown in Table 6, there was no significant difference in redness during the fermentation of the property field.
[누룩 종류에 따른 속성장의 황색도(b) 변화][Changes in yellowness (b) of properties of yeast depending on the type of yeast]
표 7은 상이한 종류의 누룩으로 제조된 속성장을 4주간 발효하여 4주간의 황색도(b) 변화를 표로 나타낸 것이다.Table 7 shows the change in yellowness (b) for 4 weeks by fermenting fast yeast made with different types of yeast for 4 weeks.
누룩 종류에 따른 속성장의 발효기간에 따른 황색도 변화를 분석한 결과 발효초기 18.93 내지 17.42에서 발효 기간이 경과함에 따라 15.58 내지 13.31로 변하였다. 상기 표 7에 나타난 바와 같이 속성장이 발효되는 동안, 황색도의 큰 차이는 없는 것으로 나타났다.As a result of analyzing the change in yellowness according to the fermentation period of the quick yeast according to the type of yeast, it changed from 18.93 to 17.42 at the beginning of fermentation to 15.58 to 13.31 as the fermentation period elapsed. As shown in Table 7, there was no significant difference in yellowness during the fermenting of the fast field.
[누룩 종류에 따른 속성장의 아미노태 질소함량변화][Changes in Amino Nitrogen Content in Instant Growth According to Types of Nuruk]
표 8은 상이한 종류의 누룩으로 제조된 속성장을 4주간 발효하여 4주간의 아미노태 질소함량변화를 표로 나타낸 것이다(단위 : mg/100g).Table 8 shows the change in amino type nitrogen content for 4 weeks by fermenting fast yeast made with different types of yeast for 4 weeks (unit: mg/100g).
아미노태 질소는 추출 시료 원액을 사용하였다. 시료 5 mL, 중성 포말린 용액 10 mL, 증류수 10 mL를 넣은 플라스크에 0.5% 페놀프탈레인 용액을 2~3 방울 가한 후, 0.05 N NaOH로 미홍색이 될 때까지의 적정량과 시료 5 mL, 증류수 20 mL를 넣은 플라스크에 0.5% 페놀프탈레인 용액을 2~3방울 가한 후, 0.05 N NaOH로 미홍색이 될 때까지의 적정량을 이용하여 아미노태 질소 함량을 산출하였다.Amino nitrogen was used as the stock solution of the extracted sample. Add 2 to 3 drops of 0.5% phenolphthalein solution to a flask containing 5 mL of sample, 10 mL of neutral formalin solution, and 10 mL of distilled water, and then titrate with 0.05 N NaOH until it turns pink, 5 mL of sample, and 20 mL of distilled water. After adding 2 to 3 drops of 0.5% phenolphthalein solution to the flask containing the mixture, the content of amino nitrogen was calculated using an appropriate amount of 0.05 N NaOH until it turned pink.
누룩 종류에 따른 속성장의 아미노태 질소함량을 분석한 결과, 발효 초기에는 74.20mg/100g 내지 116.20mg/100g이었고, 발효가 진행됨에 따라 증가하였다. 발효 4주 경과 후, 대두로 누룩은 만든 경우가 247.80mg/100g로 가장 낮은 값을 보였으며, 통밀로 누룩을 만든 경우가 425.13mg/100g으로 가장 높은 값을 나타내었다. 이에 따라, 발효가 진행됨에 따라, 아미노태 질소 함량이 늘어남을 확인하였다. 아미노태 질소는 구수한 맛을 내는 성분으로, 속성장의 맛에 중요한 역할을 한다.As a result of analyzing the amino type nitrogen content of fast fermentation according to the type of yeast, it was 74.20mg/100g to 116.20mg/100g at the beginning of fermentation, and increased as fermentation progressed. After 4 weeks of fermentation, the case of yeast made with soybeans showed the lowest value of 247.80mg/100g, and the case of yeast made of whole wheat showed the highest value of 425.13mg/100g. Accordingly, it was confirmed that as the fermentation progressed, the amino nitrogen content increased. Amino nitrogen is a savory taste component and plays an important role in the taste of fast food.
[누룩 종류에 따른 속성장의 일반 세균 수 변화][Changes in the number of general bacteria in the quick-drying yeast depending on the type of yeast]
표 9는 상이한 종류의 누룩으로 제조된 속성장을 4주간 발효하여 4주간의 일반 세균 수 변화를 표로 나타낸 것이다(단위 : Log CFU/g).Table 9 shows the change in the number of general bacteria for 4 weeks by fermenting fast yeast prepared with different types of yeast for 4 weeks (Unit: Log CFU / g).
속성장의 미생물 생균수는 Gil 등(20)의 방법에 의해서 조사되었다. 속성장 1 g에 0.85%(w/v) 생리식염수 9 mL을 시험관에 담아 균질화시키고 이를 십진희석법으로 희석하여 총균수는 Tryptic Soy Agar(BD Difco, USA), 유산균수는 (Lactobacilli MRS Agar); BD Difco, USA) 배지를 이용하여 접종 도말하였다. 총균수는 30℃에서 24시간 동안 호기배양, 유산균수는 48-72시간 동안 혐기배양 한 후 형성된 집락을 2회 반복 계수하여 log CFU/g로 환산하여 표시하였다.The number of viable microorganisms in the fast field was investigated by the method of Gil et al. (20). 9 mL of 0.85% (w / v) physiological saline solution was added to 1 g of fast-acting field in a test tube, homogenized, and diluted by decimal dilution method to determine the total number of bacteria: Tryptic Soy Agar (BD Difco, USA), the number of lactic acid bacteria (Lactobacilli MRS Agar); BD Difco, USA) medium was used to inoculate and smear. The total number of bacteria was aerobically cultured at 30 ° C for 24 hours, and the number of lactic acid bacteria was anaerobically cultured for 48-72 hours, and the colonies formed were counted twice and converted into log CFU / g.
누룩 종류에 따른 속성장의 일반 세균 수를 분석한 결과 발효 초기 6.32Log CFU/g 내지 7.02Log CFU/g에서 발효기간이 경과함에 따라 6.89Log CFU/g 내지 8.45Log CFU/g로 증가하였으며, 특히 도정수수로 만든 누룩을 첨가한 속성장에서 전반적으로 높은 값을 보였고 통밀을 누룩으로 사용한 속성장의 일반세균수가 가장 낮게 나타났다.As a result of analyzing the number of normal bacteria in the fast fermentation according to the type of yeast, it increased from 6.32 Log CFU/g to 7.02 Log CFU/g at the beginning of fermentation to 6.89 Log CFU/g to 8.45 Log CFU/g as the fermentation period elapsed, especially during milling. Overall, the high value was shown in the fast fermentation with sorghum-made yeast, and the lowest number of general bacteria was found in the rapid fermentation using whole wheat as yeast.
[누룩 종류에 따른 속성장의 유산균 수 변화][Changes in the number of lactic acid bacteria in fast-acting yeast depending on the type of yeast]
표 10은 상이한 종류의 누룩으로 제조된 속성장을 4주간 발효하여 4주간의 유산균 수 변화를 표로 나타낸 것이다(단위 : Log CFU/g).Table 10 shows the change in the number of lactic acid bacteria for 4 weeks by fermenting fast yeast prepared with different types of yeast for 4 weeks (Unit: Log CFU / g).
누룩 종류에 따른 속성장의 유산균 수를 분석한 결과 발효 초기 6.84Log CFU/g 내지 7.04Log CFU/g에서 발효기간이 경과함에 따라 7.05Log CFU/g 내지 8.44Log CFU/g로 증가하였다. 발효 후 4주 경과 시, 통밀을 누룩으로 한 속성장의 유산균 수가 7.05 Log CFU/g로 가장 낮게 나타났고, 도정수수를 누룩으로 한 속성장의 유산균 수가 8.44 Log CFU/g로 가장 높게 나타났다. As a result of analyzing the number of lactic acid bacteria in the rapid fermentation according to the type of yeast, it increased from 6.84 Log CFU / g to 7.04 Log CFU / g at the beginning of fermentation to 7.05 Log CFU / g to 8.44 Log CFU / g as the fermentation period elapsed. At 4 weeks after fermentation, the number of lactic acid bacteria in the fast-cooked broth with whole wheat as yeast was the lowest at 7.05 Log CFU/g, and the number of lactic acid bacteria in the fast-jang with milled soybean as yeast was the highest at 8.44 Log CFU/g.
[누룩 종류에 따른 속성장의 총폴리페놀 및 DPPH 라디칼 소거능(%)][Total polyphenols and DPPH radical scavenging ability (%) of rapid growth according to the type of yeast]
표 11은 상이한 종류의 누룩으로 제조된 속성장을 4주간 발효하여 발효 전 후의 총폴리페놀 함량 및 DPPH 라디칼 소거능의 변화를 표로 나타낸 것이다(단위 : Log CFU/g).Table 11 shows the changes in total polyphenol content and DPPH radical scavenging ability before and after fermentation by fermenting fast yeast prepared with different types of yeast for 4 weeks (Unit: Log CFU / g).
본 발명에 따른 총폴리페놀 함량은 폴린-시오칼투(Folin-Ciocalteu's) 방법에 따라 폴린-시오칼투(Folin-Ciocalteu) 시약이 추출물의 폴리페놀성 화합물에 의해 환원된 결과, 몰리브덴 청색으로 발색하는 것을 원리로 측정하였다(Jang 등 2012). 추출물 50μL에 2% Na2CO3 1 mL를 혼합하여 3분 방치하고 50% 폴린-시오칼투 페놀용액(Folin-Ciocalteu's phenol reagent; Sigma-Aldrich, St. Louis, MO, USA) 50 μL를 혼합하여 1시간 반응시킨 후 750 nm에서 흡광도 값을 측정하였다. 표준물질은 갈산(gallic acid; Sigma-Aldrich, USA)를 사용하여 동일한 방법으로 작성된 검량선으로부터 총 페놀 함량으로 환산하였다.The total polyphenol content according to the present invention is based on the fact that the Folin-Ciocalteu reagent is reduced by the polyphenolic compound of the extract according to Folin-Ciocalteu's method, resulting in the development of molybdenum blue color. It was measured according to the principle (Jang et al. 2012). Mix 1 mL of 2% Na 2 CO 3 with 50 μL of the extract, leave for 3 minutes, and mix with 50 μL of 50% Folin-Ciocalteu's phenol reagent (Sigma-Aldrich, St. Louis, MO, USA). After reacting for 1 hour, the absorbance value was measured at 750 nm. The standard material was converted into total phenol content from a calibration curve prepared in the same way using gallic acid (Sigma-Aldrich, USA).
본 발명에 따른 DPPH 라디칼 소거능에서의 전자공여능(Electron Donating Ability: EDA)은 DPPH(1,1-diphenyl-2-picrylhydrazyl) 방법으로 측정하였다(Choi 등 2003). 0.4 mM DPPH 용액을 흡광도 값이 1.3~1.4가 되도록 희석한 후 추출물 0.2 mL에 DPPH(Sigma-Aldrich, USA) 용액 0.8 mL를 가하여, 실온에서 30분간 방치 후 분광광도계(Cary UV-Visspectrophotometer, Agilent Technologies, Santa Clara, CA, USA)를 사용하여 525 nm에서 흡광도를 측정하였다. 흡광도를 측정할 때 셀에 분주되는 각 시료에 의한 흡광도의 차이는 증류수만의 흡광도를 측정하여 보정해 주었고, 이때 전자공여능은 시료 첨가구와 비첨가구의 흡광도 차이를 백분율(%)로 구하였다.Electron Donating Ability (EDA) in DPPH radical scavenging activity according to the present invention was measured by DPPH (1,1-diphenyl-2-picrylhydrazyl) method (Choi et al. 2003). After diluting the 0.4 mM DPPH solution to an absorbance value of 1.3 to 1.4, 0.8 mL of DPPH (Sigma-Aldrich, USA) solution was added to 0.2 mL of the extract, left at room temperature for 30 minutes, and then measured using a spectrophotometer (Cary UV-Visspectrophotometer, Agilent Technologies). , Santa Clara, CA, USA) was used to measure the absorbance at 525 nm. When measuring the absorbance, the difference in absorbance by each sample dispensed into the cell was corrected by measuring the absorbance of only distilled water, and at this time, the electron donating ability was calculated by percentage (%).
누룩 종류에 따른 속성장의 총폴리페놀 함량을 분석한 결과 발효초기에는 295.80mg/100g 내지 411.75mg/100g 범위에 속하였으며, 4주후에는 638.85mg/100g 내지 769.46mg/100g로 증가하였다. 발효 후 4주가 경과한 속성장의 경우는 특히, 수수+대두로 만든 누룩을 이용한 속성장의 총폴리페놀 함량이 769.46mg/100g로 가장 높게 나타났으며, 수수+보리로 만든 누룩을 이용한 속성장의 총폴리페놀 함량이 638.85mg/100g로 가장 낮게 나타났다. 총폴리페놀 함량은 누룩간 큰 차이가 없는 것으로 나타났으나 수수를 첨가한 2번, 3번, 6번의 수수 속성장의 총폴리페놀 함량이 높은 것으로 나타났다.누룩 종류에 따른 속성장의 DPPH 라디칼 소거능으로 살펴본 항산화성은 발효 초기에 28.81% 내지 42.89%를 나타내었으며, 4주 후에는 51.40% 내지 63.90%로 증가하는 경향을 나타내었다. 특히, 수수 누룩을 이용한 2번, 3번, 6번과 비도정 수수로 만든 콩알 메주를 사용한 속성장의 항산화성이 높은 것으로 나타났다.As a result of analyzing the total polyphenol content according to the type of yeast, it was in the range of 295.80 mg / 100 g to 411.75 mg / 100 g at the beginning of fermentation, and increased to 638.85 mg / 100 g to 769.46 mg / 100 g after 4 weeks. In the case of accelerated fermentation after 4 weeks of fermentation, in particular, the total polyphenol content of accelerated fermentation using yeast made from sorghum + soybean was the highest at 769.46mg/100g, and the total polyphenol content of accelerated fermentation using yeast made from sorghum + barley was the highest. The phenol content was the lowest at 638.85mg/100g. There was no significant difference in the total polyphenol content among yeasts, but the total polyphenol content of the sorghum fastening of No. 2, No. 3, and No. 6 with sorghum added was high. The antioxidant properties were 28.81% to 42.89% at the beginning of fermentation, and increased to 51.40% to 63.90% after 4 weeks. In particular, No. 2, No. 3, and No. 6 using sorghum nuruk and soy bean meju made from unprocessed sorghum showed high antioxidant properties.
[누룩 종류에 따른 속성장의 관능검사 결과][Sensory test result of property field according to yeast type]
표 12는 누룩 종류에 따른 속성장의 관능검사(색, 향, 짠맛, 지미, 단맛 및 기호도)를 평가한 결과를 표로 나타낸 것이다.Table 12 shows the results of evaluating the sensory tests (color, aroma, saltiness, taste, sweetness, and preference) of the attribute field according to the type of yeast.
표 12에 나타난 바와 같이 누룩 종류에 따른 속성장의 관능검사를 실시하였다. 관능검사는 충청북도 농업기술원 식품개발팀에 근무하는 7명의 관능검사원을 대상으로 발효주의 색, 향, 단맛, 지미, 전반적인 기호도를 1(very bad)에서 9(very good)까지의 점수로 평가하였다. 시험결과는 통계 package window용 SAS rel. 6.12를 사용하여 분산분석 하였으며, 시료간 차이의 유무는 Duncan's multiple range test를 사용하여 비교 분석하였다(SAS institute, 1998).관능검사 결과, 비도정 수수(콩알)를 이용한 속성장이 색, 향, 짠맛, 지미, 단맛 및 기호도의 모든 관능검사 항목에서 가장 우수한 결과를 나타내었다. As shown in Table 12, a sensory test for the fast-growing yeast was performed according to the type of yeast. For the sensory test, seven sensory inspectors working in the food development team of the Chungcheongbuk-do Agricultural Research and Extension Services evaluated the color, aroma, sweetness, taste, and overall acceptability of the fermented wine on a scale of 1 (very bad) to 9 (very good). Test results are SAS rel. 6.12 was used for analysis of variance, and the presence or absence of differences between samples was comparatively analyzed using Duncan's multiple range test (SAS institute, 1998). It showed the best results in all sensory test items such as taste, taste, sweetness and acceptability.
[수수 누룩(비도정 수수(콩알) 첨가량에 따른 속성장 배합][Sorghum yeast (according to the amount of unpolished sorghum (bean kernels) added)
표 13은 비도정 수수를 이용한 누룩의 첨가비율에 따른 속성장의 배합비를 나타낸 표이다(단위 : g).Table 13 is a table showing the blending ratio of fast soy sauce according to the addition ratio of nuruk using unpolished sorghum (unit: g).
수수 누룩은 각각 수수를 10중량%, 30중량% 또는 50중량%를 첨가하여 누룩을 제조하였다. 상기와 같이 제조된 누룩을 메주가루, 소금 및 물과 혼합하여, 속성장을 제조하였다. 수수를 10중량% 첨가하여 제조한 누룩의 경우, 누룩 70중량부, 메주가루 630중량부, 소금 200중량부 및 물 1100중량부를 첨가하여 속성장을 제조하였다. 수수를 30중량% 첨가하여 제조한 누룩의 경우, 누룩 210중량부, 메주가루 490중량부, 소금 200중량부 및 물 1100중량부를 첨가하여 속성장을 제조하였다. 수수를 50중량% 첨가하여 제조한 누룩의 경우, 누룩 350중량부, 메주가루 350중량부, 소금 200중량부 및 물 1100중량부를 첨가하여 속성장을 제조하였다.Sorghum yeast was prepared by adding 10% by weight, 30% by weight or 50% by weight of sorghum, respectively. The nuruk prepared as described above was mixed with fermented soybean flour, salt and water to prepare a quick paste. In the case of yeast prepared by adding 10% by weight of sorghum, 70 parts by weight of yeast, 630 parts by weight of fermented soybean paste, 200 parts by weight of salt and 1100 parts by weight of water were added to prepare a quick paste. In the case of yeast prepared by adding 30% by weight of sorghum, 210 parts by weight of yeast, 490 parts by weight of fermented soybean paste, 200 parts by weight of salt, and 1100 parts by weight of water were added to prepare a quick paste. In the case of yeast prepared by adding 50% by weight of sorghum, 350 parts by weight of yeast, 350 parts by weight of meju powder, 200 parts by weight of salt, and 1100 parts by weight of water were added to prepare a quick paste.
[수수 누룩(비도정 수수(콩알) 첨가량에 따른 속성장 관능검사 결과][According to sorghum yeast (non-polished sorghum (bean kernels) addition amount) sensory test result]
표 14은 비도정 수수를 이용한 누룩의 첨가비율에 따른 속성장의 관능검사 결과를 나타낸 표이다.Table 14 is a table showing the results of the sensory test for fast fermentation according to the addition ratio of nuruk using unpolished sorghum.
수수 누룩 첨가량에 따른 속성장 관능검사 결과 향과, 짠맛 및 단맛에 대한 기호도가 대두를 이용하여 제조한 누룩에 비해 선호도가 좋은 것으로 나타났으며, 전반적인 수수 누룩 첨가에 의해 높은 값을 보였다. 특히 수수 누룩 30%가 가장 높은 기호도를 나타냈다.As a result of the rapid sensory test according to the amount of sorghum nuruk added, preference for aroma, saltiness, and sweetness was found to be better than that of nuruk prepared using soybeans, and the overall value was high due to the addition of sorghum nuruk. In particular, 30% sorghum yeast showed the highest preference.
Claims (8)
분쇄된 상기 곡류를 물과 혼합하며 반죽하고 성형하는 단계;
반죽된 상기 곡류를 발효하여 누룩을 만드는 단계;
햇볕 또는 건조기를 이용하여 상기 누룩을 겉말림하는 단계;
상기 누룩을 분쇄하고, 분쇄된 상기 누룩에 메주가루, 소금 및 물을 혼합하여 속성장을 제조하는 단계; 및
상기 속성장을 발효하는 단계를 포함하고,
상기 수수가 첨가된 상기 곡류를 분쇄하는 단계는,
통밀 또는 보리 중 어느 하나 이상을 더 포함하고,
상기 성형하는 단계는,
상기 수수, 상기 통밀 또는 상기 보리 중 어느 하나 이상이 첨가된 시료와 물을 1 : 0.25 내지 1 : 2.0의 비율로 혼합하여 혼합물을 형성하는 단계; 및
상기 혼합물을 고르게 분쇄하는 단계를 포함하고,
상기 곡류를 발효하여 누룩을 만드는 단계는,
상기 누룩을 온도 20℃ 내지 40℃, 습도 40% 내지 90%에서 3일 내지 24일 발효하는 단계이며,
상기 속성장은 누룩 및 메주 가루의 중량비가 30:70이며,
상기 혼합하는 단계는,
소금 100중량부 내지 300중량부, 물 700중량부 내지 1500중량부, 메주가루 250중량부 내지 800중량부 및 누룩 50중량부 내지 450중량부를 혼합하는 단계이고,
상기 속성장을 발효하는 단계는,
20℃내지 40℃에서 20일 내지 40일 발효하는 단계인 수수 속성장 제조방법.Grinding grains to which sorghum was added;
Mixing the pulverized grains with water, kneading and shaping;
Making yeast by fermenting the kneaded grains;
Drying the nuruk using sunlight or a dryer;
Grinding the yeast, and mixing the crushed fermented soybean flour, salt and water to prepare a fast-acting paste; and
Including the step of fermenting the attribute field,
The step of grinding the grains to which the sorghum was added,
Further comprising any one or more of whole wheat or barley,
The molding step is
Forming a mixture by mixing a sample to which at least one of the sorghum, the whole wheat, or the barley is added and water at a ratio of 1:0.25 to 1:2.0; and
Evenly grinding the mixture,
The step of fermenting the grains to make yeast,
It is a step of fermenting the yeast for 3 to 24 days at a temperature of 20 ° C to 40 ° C and a humidity of 40% to 90%,
The weight ratio of yeast and meju flour is 30:70,
The mixing step is
Mixing 100 parts by weight to 300 parts by weight of salt, 700 parts by weight to 1500 parts by weight of water, 250 parts by weight to 800 parts by weight of fermented soybean paste, and 50 parts by weight to 450 parts by weight of yeast,
The step of fermenting the attribute chapter,
A method for producing sorghum fast growing, which is a step of fermenting at 20 ° C to 40 ° C for 20 to 40 days.
A sorghum fastened soybean paste prepared by the method of claim 1.
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